ICE Pharma offers a unique range of bile acid products and best-in-class services for the pharmaceutical industry.
01 1ICE S.P.A. Basaluzzo, Alessandria IT
01 1Chenodeoxycholic Acid, Product codes: 2608 - 2610 - 2611
01 1Italy
01 1Valid
ICE Pharma offers a unique range of bile acid products and best-in-class services for the pharmaceutical industry.
ICE Pharma offers a unique range of bile acid products and best-in-class services for the pharmaceutical industry.
Chenodeoxycholic Acid, Product Codes: 2608 - 261...
Certificate Number : R1-CEP 2003-238 - Rev 01
Status : Valid
Issue Date : 2020-06-05
Type : TSE
Substance Number : 1189
86
PharmaCompass offers a list of Chenodeoxycholic Acid API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Chenodeoxycholic Acid manufacturer or Chenodeoxycholic Acid supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Chenodeoxycholic Acid manufacturer or Chenodeoxycholic Acid supplier.
PharmaCompass also assists you with knowing the Chenodeoxycholic Acid API Price utilized in the formulation of products. Chenodeoxycholic Acid API Price is not always fixed or binding as the Chenodeoxycholic Acid Price is obtained through a variety of data sources. The Chenodeoxycholic Acid Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A EC 207-481-8 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of EC 207-481-8, including repackagers and relabelers. The FDA regulates EC 207-481-8 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. EC 207-481-8 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of EC 207-481-8 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A EC 207-481-8 supplier is an individual or a company that provides EC 207-481-8 active pharmaceutical ingredient (API) or EC 207-481-8 finished formulations upon request. The EC 207-481-8 suppliers may include EC 207-481-8 API manufacturers, exporters, distributors and traders.
click here to find a list of EC 207-481-8 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A EC 207-481-8 CEP of the European Pharmacopoeia monograph is often referred to as a EC 207-481-8 Certificate of Suitability (COS). The purpose of a EC 207-481-8 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of EC 207-481-8 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of EC 207-481-8 to their clients by showing that a EC 207-481-8 CEP has been issued for it. The manufacturer submits a EC 207-481-8 CEP (COS) as part of the market authorization procedure, and it takes on the role of a EC 207-481-8 CEP holder for the record. Additionally, the data presented in the EC 207-481-8 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the EC 207-481-8 DMF.
A EC 207-481-8 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. EC 207-481-8 CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of EC 207-481-8 suppliers with CEP (COS) on PharmaCompass.
We have 1 companies offering EC 207-481-8
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